Polat, R.; Ustyol, A.; Tuncez, E.; Guran, T.
(SPRINGER, 2020)
Background Allgrove syndrome (OMIM 231550) is a rare autosomal recessive disease characterized by non-CAH primary adrenal insufficiency (non-CAH PAI), alacrima, and achalasia. It is caused by mutations in the AAAS gene. ...